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Dingemans, Irene
44
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Online (44)
Mediatypes
Articles (Online) (9)
OpenAccess-fulltext (35)
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?
1
Differences in health care experiences between rare cancer ..:
de Heus, Eline
;
Engelen, Vivian
;
Dingemans, Irene
...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1186/..
?
2
Differences in health care experiences between rare cancer ..:
de Heus, Eline
;
Engelen, Vivian
;
Dingemans, Irene
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170927/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
3
Differences in health care experiences between rare cancer ..:
Eline de Heus
;
Vivian Engelen
;
Irene Dingemans
...
https://doi.org/10.1186/s13023-021-01886-2. , 2021
Link:
https://doi.org/10.1186/..
?
4
Additional file 1 of Differences in health care experiences..:
Eline de Heus (10908128)
;
Vivian Engelen (10908131)
;
Irene Dingemans (10908134)
...
https://figshare.com/articles/journal_contribution/Additional_file_1_of_Differences_in_health_care_experiences_between_rare_cancer_and_common_cancer_patients_results_from_a_national_cross-sectional_survey/14714951. , 2021
Link:
https://doi.org/10.6084/..
?
5
Optical properties of N,N′-bis(3-phenoxy-3-phenoxy-phenoxy)..:
Yang, D.
;
Shrestha, R.P.
;
Dingemans, T.J.
..
Thin Solid Films. 500 (2006) 1-2 - p. 9-14 , 2006
Link:
https://doi.org/10.1016/..
?
6
DNA methylation episignature, extension of the clinical fea..:
van der Laan, Liselot
;
Karimi, Karim
;
Rooney, Kathleen
...
Genetics in Medicine. 26 (2024) 3 - p. 101050 , 2024
Link:
https://doi.org/10.1016/..
?
7
A new blood DNA methylation signature for Koolen-de Vries s..:
Awamleh, Zain
;
Choufani, Sanaa
;
Wu, Wendy
...
European Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
8
Motives for using social networking sites: a uses & gratifi..:
Dingemans, Alexandra E.
;
Veldhuis, Jolanda
;
Lähde, Irene
Journal of Eating Disorders. 11 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
9
Missense variants in ANKRD11 cause KBG syndrome by impairme..:
de Boer, Elke
;
Ockeloen, Charlotte W.
;
Kampen, Rosalie A.
...
Genetics in Medicine. 25 (2023) 11 - p. 100962 , 2023
Link:
https://doi.org/10.1016/..
?
10
Missense variants in ANKRD11 cause KBG syndrome by impairme..:
de Boer, Elke
;
Ockeloen, Charlotte W.
;
Kampen, Rosalie A.
...
Genetics in Medicine. 24 (2022) 10 - p. 2051-2064 , 2022
Link:
https://doi.org/10.1016/..
?
11
In‐depth molecular analysis of combined and co‐primary pulm..:
Hermans, Bregtje C. M.
;
Derks, Jules L.
;
Hillen, Lisa M.
...
International Journal of Cancer. 150 (2021) 5 - p. 802-815 , 2021
Link:
https://doi.org/10.1002/..
?
12
Cardiac pathology in neuronal ceroid lipofuscinoses —a clin..:
Ofman, Irene L.
;
Van Der Wal, Allard C.
;
Dingemans, Koert P.
.
European Journal of Paediatric Neurology. 5 (2001) - p. 213-217 , 2001
Link:
https://doi.org/10.1053/..
?
13
Missense variants in ANKRD11 cause KBG syndrome by impairme..:
de Boer, Elke
;
Ockeloen, Charlotte
;
Kampen, Rosalie
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2022.06.007. , 2022
Link:
https://univ-rennes.hal...
?
14
Missense variants in ANKRD11 cause KBG syndrome by impairme..:
de Boer, Elke
;
Ockeloen, Charlotte
;
Kampen, Rosalie
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2022.06.007. , 2022
Link:
https://univ-rennes.hal...
?
15
Missense variants in ANKRD11 cause KBG syndrome by impairme..:
de Boer, Elke
;
Ockeloen, Charlotte
;
Kampen, Rosalie
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.gim.2022.06.007. , 2022
Link:
https://univ-rennes.hal...
1-15